A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv954n54



Internal ID22768849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9011080..9066580hg38UCSC Ensembl
chr10:9053043..9108543hg19UCSC Ensembl
chr10:9093049..9148549hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3855501
hg1955501
hg1855501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549955, nsv549954
SamplesHGDP00021
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv954n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer